Abstract
We present the case of a 6-year-old boy who had an omphalocele repaired at day 1 of life. He had a secundum atrial septal defect and an anomalous inferior vena cava of a type which has not been previously reported. Cine-MRI was a useful noninvasive tool for diagnosing the anomalous subaortic innominate vein and four immature vessels which make up the venous drainage systems of the lumbar region. The recognition of this malformation is important in planning and executing surgical repair or cardiac catheterization for postoperative patients with omphaloceles.
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References
Dillon PW, Cilley RE (1993) Newborn surgical emergencies (gastro-intestinal anomalies, abdominal wall defects). In: Altman PR, Stylianos S (eds) Pediatric Clinics of North America. Saunders, Philadelphia, pp 1207–1210
Greenwold RD, Rosenthal A, Nadas AS (1974) Cardiovascular malformations associated with omphalocele. J Pediatr 85:818–821
Onouchi Z, Ootsuka T, Otabe E, Sasakawa H, Takeda Y, Goto M (1975) A case of omphalocele. Jpn Heart J 16:211–220
Gorenstein A, Meyer S, Schiller M (1983) Inferior vena cava anomalies associated with gaint omphalocele. A proposed classification. Z Kinderchir 38:380–382
Waldman JD, Fellows KE, Paul MH, Muster AJ (1977) Angulation of IVC-RA junction in children with repaired omphalocele. Pediatr Radiol 5:142–144
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Antoniou, E.E.H., Matsuoka, S., Mori, K. et al. Anomalous inferior vena cava in association with omphalocele: A case report. Pediatr Radiol 25, 265–266 (1995). https://doi.org/10.1007/BF02011095
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DOI: https://doi.org/10.1007/BF02011095